Le lymphœdème congénital primaire: la maladie de Milroy: à propos du premier cas observé dans le Département de Pédiatrie du Centre Hospitalier Universitaire Yalgado Ouédraogo, Ouagadougou

Congenital lymphedema is the accumulation of lymphatic fluid in the child’s interstitial spaces. Milroy disease is a rare, hereditary, autosomal dominant condition showing incomplete penetrance. We report the case of a 7-year old little girl with Milroy disease examined for erysipelas on congenital...

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Detalles Bibliográficos
Autores principales: Ouattara, Chantal Zoungrana, Kalmogho, Angèle, Yonaba, Caroline, Bouda, Chantal Gabrielle, Yaméogo, Ghislaine, Kam, Ludovic
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511709/
https://www.ncbi.nlm.nih.gov/pubmed/28748022
http://dx.doi.org/10.11604/pamj.2017.27.21.11443

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511709/
https://www.ncbi.nlm.nih.gov/pubmed/28748022
http://dx.doi.org/10.11604/pamj.2017.27.21.11443

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